ライフサイエンスコーパス: Helianthus annuus

1 ion and modern improvement of the sunflower (Helianthus annuus).

2 eloping seeds of two genotypes of sunflower (Helianthus annuus).

3 ri), squash (Cucurbita pepo), and sunflower (Helianthus annuus).

4 Sunflower (Helianthus annuus), a moderately salt-tolerant crop, exh

5 Helianthus annuus, a highly outcrossing species, is mark

6 traits distinguishing two annual sunflowers, Helianthus annuus and H. debilis ssp. cucumerifolius.

7 ids between two species of Texas sunflowers (Helianthus annuus and H. debilis) that form a natural hy

8 ackcross between two wild annual sunflowers, Helianthus annuus and H. petiolaris, interpret different

9 tion between the sympatric sunflower species Helianthus annuus and H. petiolaris.

10 rypsin-inhibitory loops exist in sunflowers (Helianthus annuus) and frogs.

11 report that leaf water washes of sunflower (Helianthus annuus) and jimson weed (Datura metel), but n

12 synteny analysis with the annual sunflower (Helianthus annuus) and lettuce (Lactuca sativa) genomes.

13 with experiments performed with sunflower ( Helianthus annuus) and wheat ( Triticum aestivum) cultiv

14 bis sativa), Pumpkin (Cucurbita), Sunflower (Helianthus annuus), and Safflower (Carthamus tinctorius)

15 a in Tradescantia pallida, Lactuca serriola, Helianthus annuus, and Oenothera caespitosa.

16 es with bundle sheath extensions, sunflower [Helianthus annuus] and dwarf bean [Phaseolus vulgaris];

17 The studies primarily used wild Helianthus annuus, but also included a commercial and ea

18 ), tomato (Solanum lycopersicum), sunflower (Helianthus annuus), Catharanthus roseus, maize (Zea mays

19 class of sesquiterpenes isolated mostly from Helianthus annuus, commonly known as sunflower.

20 The common sunflower (Helianthus annuus) contains the unusual gene PawS1 (Prep

21 pathogen, we analyzed transgenic sunflower (Helianthus annuus cv SMF3) plants constitutively express

22 g that a frameshift mutation in one paralog, Helianthus annuus FT 1 (HaFT1), underlies a major QTL fo

23 lupin (Lupin angustifolius), and sunflower (Helianthus annuus) grew well at 100 microm Mn.

24 ohistoric data demonstrating that sunflower (Helianthus annuus) had entered the repertoire of Mexican

25 al adaptation in three species of sunflower: Helianthus annuus, Helianthus argophyllus, and Helianthu

26 encing 1,506 wild sunflowers from 3 species (Helianthus annuus, Helianthus petiolaris and Helianthus

27 ran herbivore, we hydroponically manipulated Helianthus annuus host plants' tissue-sodium concentrati

28 originating from the wild sunflower species Helianthus annuus, is able to restore the widely used PE

29 f the thermally induced VPs in the leaves of Helianthus annuus L. seedlings in situ.

30 mance trials of oilseed sunflower varieties (Helianthus annuus L.) conducted since 1978 across the Gr

31 Genetic diversity in modern sunflower (Helianthus annuus L.) cultivars (elite oilseed inbred li

32 e now debated, and until recently sunflower (Helianthus annuus L.) has been considered the only undis

33 , we immersed marked, decapitated sunflower (Helianthus annuus L.) hypocotyl sections in buffered aux

34 Sunflower (Helianthus annuus L.) production is challenged by differ

35 To date, the domestication of sunflower (Helianthus annuus L.) stands as the only counterexample

36 the most devastating diseases of sunflower (Helianthus annuus L.), affecting global production.

37 g seedlings of cocklebur, tomato, sunflower (Helianthus annuus L.), and soybean (Glycine max [L.] Mer

38 amics of transposable elements in sunflower (Helianthus annuus L.), especially given its large genome

39 tion (GWA) analyses in cultivated sunflower (Helianthus annuus L.).

40 Rf1 is used for commercial hybrid sunflower (Helianthus annuus L., 2n = 34) seed production worldwide

41 The domesticated sunflower, Helianthus annuus L., is a global oil crop that has prom

42 nucleus) of the first leaf of the sunflower, Helianthus annuus L., is influenced by the quality and t

43 capacity in sun- and shade-grown sunflower (Helianthus annuus) leaves underlies its previously obser

44 n: acacia (Robinia pseudoacacia), sunflower (Helianthus annuus), linden (Tilia cordata), basil (Ocimu

45 ve (i.e., landrace), and improved sunflower (Helianthus annuus) lines.

46 ntained the rbcL gene from either sunflower (Helianthus annuus) or the cyanobacterium Synechococcus P

47 For instance, in Allium cepa, Helianthus annuus, or Andropogon gerardi, more than 35%

48 Here, we report the 3D NMR structure of the Helianthus annuus PawS1 (preproalbumin with sunflower tr

49 ylem anatomy and resistance to cavitation in Helianthus annuus plants grown under three CO(2) regimes

50 Brassica napus and Helianthus annuus pollen were the variables situated nea

51 gene expression between two wild (non-weedy) Helianthus annuus populations from Utah and Kansas and f

52 nspired by the traditional use of sunflower (Helianthus annuus) preparations for analgesic purposes,

53 ommunis, Arabidopsis [Arabidopsis thaliana], Helianthus annuus, Solanum lycopersicum, and Beta vulgar

54 ach is demonstrated on leaves of sunflowers (Helianthus annuus), soy beans (Glycine max), and corn (Z

55 Heiser hypothesized that Helianthus annuus ssp. texanus was derived by the introd

56 xylem (Populus angustifolia, P. tremuloides, Helianthus annuus stems, and Aesculus hippocastanum peti

57 We grew 33 sunflower (Helianthus annuus) strains (n = 5) that varied in their

58 ion at 128 EST-based microsatellites in wild Helianthus annuus, using populations from the species' t

59 lder (Iva annua var. macrocarpa), sunflower (Helianthus annuus var. macrocarpus), and 2 cultivated va

60 the leaf surface of the heterobaric species Helianthus annuus was covered by 4-mm-diameter patches o